Delamination resistant pharmaceutical glass containers containing active pharmaceutical ingredients

US9707155B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9707155-B2
Application numberUS-201414259286-A
CountryUS
Kind codeB2
Filing dateApr 23, 2014
Priority dateApr 24, 2013
Publication dateJul 18, 2017
Grant dateJul 18, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention is based, at least in part, on the identification of a pharmaceutical container formed, at least in part, of a glass composition which exhibits a reduced propensity to delaminate, i.e., a reduced propensity to shed glass particulates. As a result, the presently claimed containers are particularly suited for storage of pharmaceutical compositions and, specifically, a pharmaceutical solution comprising a pharmaceutically active ingredient, for example, LYXUMIA (lixisenatide), LEMTRADA (alemtuzumab), REGN727/SAR236553 (alirocumab), SAR2405550/BSI-201 (iniparib), OTAMIXABAN (otamixaban), SARILUMAB (sarilumab), LANTUS and LYXUMIA (insulin glargine and lixisenatide) or VISAMERIN/MULSEVO (semuloparin sodium).

First claim

Opening claim text (preview).

What is claimed is: 1. A pharmaceutical product comprising: lixisenatide, alemtuzumab, alirocumab, iniparib, otamixaban, sarilumab, insulin glargine and lixisenatide or semuloparin sodium and a pharmaceutically acceptable excipient; contained within a glass pharmaceutical container comprising a glass composition comprising: SiO 2 in a an amount greater than or equal to about 72 mol. % and less than or equal to about 78 mol. %; alkaline earth oxide comprising both MgO and CaO, wherein CaO is present in an amount up to about 1.0 mol. %, and a ratio (CaO (mol. %)/(CaO (mol. %)+MgO (mol. %))) is less than or equal to 0.5; X mol. % Al 2 O 3 , wherein X is greater than or equal to about 5 mol. % and less than or equal to about 7 mol. %; Y mol. % alkali oxide, wherein the alkali oxide comprises Na 2 O in an amount greater than about 8 mol. %; and a ratio of a concentration of B 2 O 3 (mol. %) in the glass container to (Y mol. %-X mol. %) is less than or equal to 0.3. 2. The pharmaceutical product of claim 1 , wherein the pharmaceutical container comprises a compressive stress greater than or equal to 150 MPa. 3. The pharmaceutical product of claim 1 , wherein the pharmaceutical container comprises a compressive stress greater than or equal to 250 MPa. 4. The pharmaceutical product of claim 1 , wherein the pharmaceutical container comprises a depth of layer greater than 30 μm. 5. The pharmaceutical product of claim 1 , wherein the pharmaceutical product comprises increased stability, product integrity, or efficacy. 6. The pharmaceutical product of claim 1 : wherein the glass pharmaceutical container has a compressive stress greater than or equal to 150 MPa and a depth of layer greater than 10 μm, and wherein the pharmaceutical product comprises increased stability, product integrity, or efficacy. 7. The pharmaceutical product of claim 1 : wherein the glass pharmaceutical container which is substantially free of boron, and wherein the pharmaceutical product comprises increased stability, product integrity, or efficacy. 8. The pharmaceutical product of claim 7 , wherein the glass pharmaceutical container comprises a compressive stress greater than or equal to 150 MPa and a depth of layer greater than 25 μm. 9. The pharmaceutical product of claim 8 , wherein the glass pharmaceutical container comprises a compressive stress greater than or equal to 300 MPa and a depth of layer greater than 35 μm. 10. The pharmaceutical product of claim 7 , wherein said glass pharmaceutical container comprises a substantially homogeneous inner layer. 11. The pharmaceutical product of claim 10 , wherein said glass pharmaceutical container comprises a compressive stress greater than or equal to 150 MPa and a depth of layer greater than 25 μm. 12. The pharmaceutical product of claim 1 , wherein the pharmaceutical container comprises an internal homogeneous layer.

Assignees

Inventors

Classifications

  • to perform ion-exchange between alkali ions (C03C21/005 takes precedence) · CPC title

  • Pyridinium derivatives, e.g. pralidoxime, pyridostigmine · CPC title

  • having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol · CPC title

  • containing calcium oxide, e.g. common sheet or container glass · CPC title

  • IL-6 · CPC title

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Frequently asked questions

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What does patent US9707155B2 cover?
The present invention is based, at least in part, on the identification of a pharmaceutical container formed, at least in part, of a glass composition which exhibits a reduced propensity to delaminate, i.e., a reduced propensity to shed glass particulates. As a result, the presently claimed containers are particularly suited for storage of pharmaceutical compositions and, specifically, a pharma…
Who is the assignee on this patent?
Corning Inc
What technology area does this patent fall under?
Primary CPC classification C03C4/20. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).